Muscle Disease. Pathology and Genetics. 2nd Edition

  • ID: 2331000
  • Book
  • 392 Pages
  • John Wiley and Sons Ltd
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Written by more than 60 international experts in the field, Muscle Disease embodies the explosion of new concepts and information on the pathology and genetics of muscle disease that has occurred in recent years.

In order to accommodate the new complex principles involved, the book is organized around the motor unit and the inherited disorders, in particular, are centered on the ultrastructure and organelles within the muscle fiber.  In this way, the wide spectrum of muscle diseases, ranging from neurogenic and inflammatory disorders to those involving defects in a single gene, can be expressed in a logical sequence.  For example, disorders that principally involve specific organelles or particular metabolic processes are grouped together, with sections on disorders of the sarcolemma, mitochondria, myofibrils, glycogen and lipid metabolism, etc.  Firm reference to clinical aspects and classification of muscle diseases has been maintained throughout the book with an initial clinical overview and with specific clinical sections in each chapter.  For ease of navigation through the complex variety of muscle diseases, each chapter has been organized in a standard pattern that allows the reader to easily locate information on individual disease entities in different chapters.

This new edition of Muscle Disease: Pathology and Genetics will be a very valuable resource for clinicians, pathologists, geneticists and basic neuroscientists involved in diagnosis, research, treatment and management of patients with muscle disease.

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List of Contributors, vii

Preface, xi

List of Abbreviations, xiii

1 Introduction to Muscle Disease: Pathology and Genetics, 1Hans H. Goebel, Caroline A. Sewry and Roy O. Weller

Section 1: Assessment of Muscle Disease

2 Clinical Features of Muscle Disease, 6Marianne de Visser

3 General Pathology of Muscle Disease, 19Caroline A. Sewry and Hans H. Goebel

4 Genetics of Muscle Disease, 39Kristen J. Nowak, Phillipa J. Lamont, and Nigel G. Laing

Section 2: Neurogenic Muscle Disease

5 Neurogenic Muscle Pathology, 68Hannes Vogel

Section 3: Diseases of Neuromuscular Transmission

6 Autoimmune Myasthenias, 78Saiju Jacob and Angela Vincent

7 Congenital Myasthenic Syndromes, 86Amina Chaouch and Hanns Lochmüller

Section 4: Sarcolemma: Muscular Dystrophies and Related Disorders

8 Dystrophin and Its Associated Glycoprotein Complex, 95Rita Barresi and Susan C. Brown

9 Proteins of the Extracellular Matrix, 102Cecilia Jimenez–Mallebrera, A. Reghan Foley, and Carsten G. Bönnemann

10 Plasma Membrane Proteins: Dysferlin, Caveolin, PTRF/Cavin, Integrin 7, and Integrin 9, 108Volker Straub, Liesbeth De Waele, and Rita Barresi

11 Sarcolemmal Ion Channelopathies, 118Karin Jurkat–Rott and Frank Lehmann–Horn

Section 5: Disorders of Nuclear Proteins and Nuclear Positioning

12 Proteins of the Nuclear Membrane and Matrix, 126Antje Bornemann

13 Centronuclear Myopathies, 134Norma Beatriz Romero and Jocelyn Laporte

Section 6: Early– and Late–Onset Disorders of Myofibrils

14 Thin Filament Proteins: Nemaline and Related Congenital Myopathies, 145Michael W. Lawlor and Alan H. Beggs

15 Nebulin: Nemaline Myopathies and Associated Disorders, 152Carina Wallgren–Pettersson, Hannu Kalimo, and Martin Lammens16 Myosins, 157Anders Oldfors

17 Disorders Caused by Mutant Z–disk Proteins, 163Montse Olivé, Isidro Ferrer, and Lev G. Goldfarb

18 Titin–related Distal Myopathies, 171Bjarne Udd

19 Scapuloperoneal Disorders and Reducing Body Myopathy Associated with the Four and Half LIM Domain Protein 1, 175Joachim Schessl

Section 7: Disorders Associated with Intermediate Filaments

20 Desminopathies, 178Rolf Schröder and Christoph S. Clemen

21 Plectinopathies, 185Lilli Winter, Rolf Schröder, and Gerhard Wiche

Section 8: Mitochondria

22 Mitochondrial Myopathies, 193Anders Oldfors

Section 9: Sarcoplasmic Reticulum and T–tubules

23 Core Myopathies, Malignant Hyperthermia Susceptibility, and Brody Disease, 214Heinz Jungbluth

Section 10: Cytoplasmic Proteins

24 Enzymes: Cytosolic Proteins Calpain–3, SEPN1, and GNE, 225Volker Straub, Liesbeth De Waele, and Rita Barresi

25 Proteins of Autophagy: LAMP–2, VMA21, VCP, and TRIM32, 234May Christine V. Malicdan and Ichizo Nishino

26 Chaperone Proteins, 246Kristl G. Claeys and Joachim Weis

27 Kelch Proteins, 252Kyle S. Yau, Montse Olivé, Phillipa J. Lamont, and Nigel G. Laing

Section 11: Metabolic and Storage Disorders

28 Disorders of Muscle Glycogen Metabolism, 254John Vissing

29 Disorders of Lipid Metabolism, 265Wen–Chen Liang and Ichizo Nishino

Section 12: Muscle Diseases with DNA Expansions

30 Myotonic Dystrophies Type 1 and 2, 273Benedikt Schoser

31 Oculopharyngeal Muscular Dystrophy, 284Bernard Brais

Section 13: Facioscapulohumeral Dystrophy

32 Facioscapulohumeral Dystrophy, 288Kevin M. Flanigan and Scott Q. Harper

Section 14: Inflammatory Myopathies

33 Polymyositis, Dermatomyositis, and Inclusion Body Myositis, 298Janice L. Holton, Lucy R. Wedderburn, and Michael G. Hanna

34 Muscle Involvement in Connective Tissue Disorders: Polyarteritis, Rheumatoid Arthritis, Systemic Lupus Erythematosus, Systemic Sclerosis, and Sjögren Syndrome, 313Elisabeth J. Rushing

35 Granulomatous and Other Immune–mediated Myopathies, 316Werner Stenzel

36 Muscle Disorders Associated with Infections, 321Leila Chimelli and Ana Lia Taratuto

Section 15: Toxic Myopathies

37 Reactions of Muscle to Toxins and Drugs, 328Eleonora Aronica and Werner Stenzel

Section 16: Aging and Systemic Disease

38 Muscle Disease Associated with Age and Systemic Disorders, 339Hannes Vogel

Section 17: Rare Structural Abnormalities

39 Disorders of Muscle with Rare Structural Abnormalities, 351Hans H. Goebel, Mehar C. Sharma, Ana Lia Taratuto, and Kristl G. Claeys

Index, 361

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This comprehensive hardback book is divided into 17 sections and has 62 highly regarded contributors from around the world.   (Neuropathology & Applied Neurobiology, 1 July 2014)

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